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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02429076
Other study ID # 2015P000566
Secondary ID
Status Withdrawn
Phase Phase 1/Phase 2
First received April 8, 2015
Last updated August 1, 2017
Start date June 2017
Est. completion date December 2019

Study information

Verified date August 2017
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to test the hypothesis that methylphenidate actively induces emergence from propofol and sevoflurane general anesthesia in healthy volunteers.


Description:

Basic science and clinical data suggest that activation of one or more of the brain's arousal pathways is a highly plausible way to induce active emergence from general anesthesia. The investigators have compelling experimental data demonstrating that methylphenidate is highly effective in actively inducing emergence from isoflurane and propofol general anesthesia in rodents. The available literature suggests that IV methylphenidate would be safe to administer to patients recovering from general anesthesia, and that in addition to promoting arousal, it would enhance breathing. Both of these effects would be highly desirable in patients recovering from general anesthesia.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2019
Est. primary completion date July 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 36 Years
Eligibility Inclusion Criteria:

1. Age 18-36 years

2. ASA classification 1 or 2

3. Normal body weight, BMI = 30

4. Non-smoker

5. Right handed

6. No history of taking stimulants

Exclusion Criteria:

- In general, patients will be excluded from the study if the state of their chronic health problems gives them an ASA physical status classification of 3 or beyond.

Study Design


Related Conditions & MeSH terms

  • Active Emergence From General Anesthesia

Intervention

Drug:
IV methylphenidate
IV methylphenidate will be administered to induce emergence from general anesthesia.
Placebo
normal saline
Sevoflurane
Inhaled anesthetic
Propofol
IV anesthetic

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Response to methlyphenidate administration The number of minutes from the administration of methylphenidate until subjects respond to verbal commands minutes to response, expected average is less than 10 minutes